The effect of asphyxia on the pharmacokinetics of ceftazidime in the term newborn
The multiple-dose pharmacokinetics of ceftazidime (CAZ) (administered twice daily in a 50 mg/kg of body weight i.v. dose) were studied in 10 severely asphyxiated term infants with suspected septicemia on d 3 of life. Nine term infants with suspected septicemia but without asphyxia served as controls...
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Veröffentlicht in: | Pediatric research 1995-11, Vol.38 (5), p.808-811 |
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description | The multiple-dose pharmacokinetics of ceftazidime (CAZ) (administered twice daily in a 50 mg/kg of body weight i.v. dose) were studied in 10 severely asphyxiated term infants with suspected septicemia on d 3 of life. Nine term infants with suspected septicemia but without asphyxia served as controls. Blood samples were collected from an arterial catheter at 0, 0.5, 1, 2, 4, 8, and 12 h after an i.v. bolus injection. A high performance liquid chromatography method was used to determine CAZ concentrations from serum. CAZ pharmacokinetics followed a one-compartment open model. The GFRs of all infants were simultaneously studied by means of the 24-h continuous inulin infusion technique. Elimination serum half-life (5.86 +/- 1.13 h versus 3.85 +/- 0.40 h) and serum trough concentrations (46 +/- 14 mg/L versus 23 +/- 7 mg/L) of CAZ were significantly (p < 0.001) increased in the asphyxiated newborn, whereas total body clearance of CAZ (128.4 +/- 25.1 mL/h versus 205.7 +/- 55.4 mL/h), CAZ clearance per kg (40.9 +/- 6.1 mL/h/kg versus 60.8 +/- 8.3 mL/h/kg), and the GFR expressed in mL/min (3.14 +/- 0.43 versus 4.73 +/- 0.89) were significantly (p < 0.001) decreased in the asphyxiated newborn. We conclude that twice daily administration of 50 mg/kg of body weight CAZ given to asphyxiated term newborns in the first days of life results in significantly higher serum trough levels in comparison with control infants. The impaired CAZ clearance is a result of a significantly decreased GFR. |
doi_str_mv | 10.1203/00006450-199511000-00028 |
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N ; VAN DER HEIJDEN, B. J ; HOP, W. C. J ; SCHOEMAKER, R. C ; BROERSE, H. M ; NEIJENS, H. J ; DE GROOT, R</creator><creatorcontrib>VAN DEN ANKER, J. N ; VAN DER HEIJDEN, B. J ; HOP, W. C. J ; SCHOEMAKER, R. C ; BROERSE, H. M ; NEIJENS, H. J ; DE GROOT, R</creatorcontrib><description>The multiple-dose pharmacokinetics of ceftazidime (CAZ) (administered twice daily in a 50 mg/kg of body weight i.v. dose) were studied in 10 severely asphyxiated term infants with suspected septicemia on d 3 of life. Nine term infants with suspected septicemia but without asphyxia served as controls. Blood samples were collected from an arterial catheter at 0, 0.5, 1, 2, 4, 8, and 12 h after an i.v. bolus injection. A high performance liquid chromatography method was used to determine CAZ concentrations from serum. CAZ pharmacokinetics followed a one-compartment open model. The GFRs of all infants were simultaneously studied by means of the 24-h continuous inulin infusion technique. Elimination serum half-life (5.86 +/- 1.13 h versus 3.85 +/- 0.40 h) and serum trough concentrations (46 +/- 14 mg/L versus 23 +/- 7 mg/L) of CAZ were significantly (p < 0.001) increased in the asphyxiated newborn, whereas total body clearance of CAZ (128.4 +/- 25.1 mL/h versus 205.7 +/- 55.4 mL/h), CAZ clearance per kg (40.9 +/- 6.1 mL/h/kg versus 60.8 +/- 8.3 mL/h/kg), and the GFR expressed in mL/min (3.14 +/- 0.43 versus 4.73 +/- 0.89) were significantly (p < 0.001) decreased in the asphyxiated newborn. We conclude that twice daily administration of 50 mg/kg of body weight CAZ given to asphyxiated term newborns in the first days of life results in significantly higher serum trough levels in comparison with control infants. The impaired CAZ clearance is a result of a significantly decreased GFR.</description><identifier>ISSN: 0031-3998</identifier><identifier>EISSN: 1530-0447</identifier><identifier>DOI: 10.1203/00006450-199511000-00028</identifier><identifier>PMID: 8552453</identifier><identifier>CODEN: PEREBL</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Asphyxia Neonatorum - metabolism ; Biological and medical sciences ; Ceftazidime - pharmacokinetics ; Emergency and intensive care: neonates and children. Prematurity. Sudden death ; Humans ; Infant, Newborn ; Intensive care medicine ; Medical sciences</subject><ispartof>Pediatric research, 1995-11, Vol.38 (5), p.808-811</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-a2f4f2bb56d2a8fff4ac4dd35ecd17db3da8fd1978237e37f7896337ec7842823</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2892787$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8552453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>VAN DEN ANKER, J. N</creatorcontrib><creatorcontrib>VAN DER HEIJDEN, B. J</creatorcontrib><creatorcontrib>HOP, W. C. J</creatorcontrib><creatorcontrib>SCHOEMAKER, R. C</creatorcontrib><creatorcontrib>BROERSE, H. M</creatorcontrib><creatorcontrib>NEIJENS, H. J</creatorcontrib><creatorcontrib>DE GROOT, R</creatorcontrib><title>The effect of asphyxia on the pharmacokinetics of ceftazidime in the term newborn</title><title>Pediatric research</title><addtitle>Pediatr Res</addtitle><description>The multiple-dose pharmacokinetics of ceftazidime (CAZ) (administered twice daily in a 50 mg/kg of body weight i.v. dose) were studied in 10 severely asphyxiated term infants with suspected septicemia on d 3 of life. Nine term infants with suspected septicemia but without asphyxia served as controls. Blood samples were collected from an arterial catheter at 0, 0.5, 1, 2, 4, 8, and 12 h after an i.v. bolus injection. A high performance liquid chromatography method was used to determine CAZ concentrations from serum. CAZ pharmacokinetics followed a one-compartment open model. The GFRs of all infants were simultaneously studied by means of the 24-h continuous inulin infusion technique. Elimination serum half-life (5.86 +/- 1.13 h versus 3.85 +/- 0.40 h) and serum trough concentrations (46 +/- 14 mg/L versus 23 +/- 7 mg/L) of CAZ were significantly (p < 0.001) increased in the asphyxiated newborn, whereas total body clearance of CAZ (128.4 +/- 25.1 mL/h versus 205.7 +/- 55.4 mL/h), CAZ clearance per kg (40.9 +/- 6.1 mL/h/kg versus 60.8 +/- 8.3 mL/h/kg), and the GFR expressed in mL/min (3.14 +/- 0.43 versus 4.73 +/- 0.89) were significantly (p < 0.001) decreased in the asphyxiated newborn. We conclude that twice daily administration of 50 mg/kg of body weight CAZ given to asphyxiated term newborns in the first days of life results in significantly higher serum trough levels in comparison with control infants. The impaired CAZ clearance is a result of a significantly decreased GFR.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Asphyxia Neonatorum - metabolism</subject><subject>Biological and medical sciences</subject><subject>Ceftazidime - pharmacokinetics</subject><subject>Emergency and intensive care: neonates and children. Prematurity. Sudden death</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><issn>0031-3998</issn><issn>1530-0447</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kFlLAzEUhYMotVZ_gpAH8W00a5N5lOIGBRHqc8hkodHZTKZo_fWmduyFkHvvOSeBDwCI0Q0miN6iXHPGUYHLkmOcpyIfIo_AFHOaB8bEMZgiRHFBy1KegrOU3hHCjEs2ARPJOWGcTsHrau2g896ZAXYe6tSvt99Bw66FQ1b6tY6NNt1HaN0QTNp5jPOD_gk2NA6GvW1wsYGt-6q62J6DE6_r5C7GewbeHu5Xi6di-fL4vLhbFoZJNhSaeOZJVfG5JVp675k2zFrKnbFY2IravLW4FJJQ4ajwQpZzmlsjJCN5OQPX-3f72H1uXBpUE5Jxda1b122SErk4yZEZkHujiV1K0XnVx9DouFUYqR1N9U9THWiqP5o5ejn-sakaZw_BEV_Wr0ZdJ6NrH3VrQjrYiCyJkIL-AjBWfOg</recordid><startdate>19951101</startdate><enddate>19951101</enddate><creator>VAN DEN ANKER, J. N</creator><creator>VAN DER HEIJDEN, B. J</creator><creator>HOP, W. C. J</creator><creator>SCHOEMAKER, R. C</creator><creator>BROERSE, H. M</creator><creator>NEIJENS, H. J</creator><creator>DE GROOT, R</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19951101</creationdate><title>The effect of asphyxia on the pharmacokinetics of ceftazidime in the term newborn</title><author>VAN DEN ANKER, J. N ; VAN DER HEIJDEN, B. J ; HOP, W. C. J ; SCHOEMAKER, R. C ; BROERSE, H. M ; NEIJENS, H. J ; DE GROOT, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-a2f4f2bb56d2a8fff4ac4dd35ecd17db3da8fd1978237e37f7896337ec7842823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Asphyxia Neonatorum - metabolism</topic><topic>Biological and medical sciences</topic><topic>Ceftazidime - pharmacokinetics</topic><topic>Emergency and intensive care: neonates and children. Prematurity. Sudden death</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VAN DEN ANKER, J. N</creatorcontrib><creatorcontrib>VAN DER HEIJDEN, B. J</creatorcontrib><creatorcontrib>HOP, W. C. J</creatorcontrib><creatorcontrib>SCHOEMAKER, R. C</creatorcontrib><creatorcontrib>BROERSE, H. M</creatorcontrib><creatorcontrib>NEIJENS, H. J</creatorcontrib><creatorcontrib>DE GROOT, R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VAN DEN ANKER, J. N</au><au>VAN DER HEIJDEN, B. J</au><au>HOP, W. C. J</au><au>SCHOEMAKER, R. C</au><au>BROERSE, H. M</au><au>NEIJENS, H. J</au><au>DE GROOT, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of asphyxia on the pharmacokinetics of ceftazidime in the term newborn</atitle><jtitle>Pediatric research</jtitle><addtitle>Pediatr Res</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>38</volume><issue>5</issue><spage>808</spage><epage>811</epage><pages>808-811</pages><issn>0031-3998</issn><eissn>1530-0447</eissn><coden>PEREBL</coden><abstract>The multiple-dose pharmacokinetics of ceftazidime (CAZ) (administered twice daily in a 50 mg/kg of body weight i.v. dose) were studied in 10 severely asphyxiated term infants with suspected septicemia on d 3 of life. Nine term infants with suspected septicemia but without asphyxia served as controls. Blood samples were collected from an arterial catheter at 0, 0.5, 1, 2, 4, 8, and 12 h after an i.v. bolus injection. A high performance liquid chromatography method was used to determine CAZ concentrations from serum. CAZ pharmacokinetics followed a one-compartment open model. The GFRs of all infants were simultaneously studied by means of the 24-h continuous inulin infusion technique. Elimination serum half-life (5.86 +/- 1.13 h versus 3.85 +/- 0.40 h) and serum trough concentrations (46 +/- 14 mg/L versus 23 +/- 7 mg/L) of CAZ were significantly (p < 0.001) increased in the asphyxiated newborn, whereas total body clearance of CAZ (128.4 +/- 25.1 mL/h versus 205.7 +/- 55.4 mL/h), CAZ clearance per kg (40.9 +/- 6.1 mL/h/kg versus 60.8 +/- 8.3 mL/h/kg), and the GFR expressed in mL/min (3.14 +/- 0.43 versus 4.73 +/- 0.89) were significantly (p < 0.001) decreased in the asphyxiated newborn. We conclude that twice daily administration of 50 mg/kg of body weight CAZ given to asphyxiated term newborns in the first days of life results in significantly higher serum trough levels in comparison with control infants. The impaired CAZ clearance is a result of a significantly decreased GFR.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>8552453</pmid><doi>10.1203/00006450-199511000-00028</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Asphyxia Neonatorum - metabolism Biological and medical sciences Ceftazidime - pharmacokinetics Emergency and intensive care: neonates and children. Prematurity. Sudden death Humans Infant, Newborn Intensive care medicine Medical sciences |
title | The effect of asphyxia on the pharmacokinetics of ceftazidime in the term newborn |
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